Structure Information
Structure

Compound Identification

SMILES

[Cu++].CCCCCOC1=C(SC2=CC=CC=C2)C(SC2=CC=CC=C2)=C(OCCCCC)C2=C1C1=NC3=NC(=NC4=C5C(=C([N-]4)N=C4N=C(N=C2[N-]1)C1=C4C(OCCCCC)=C(SC2=CC=CC=C2)C(SC2=CC=CC=C2)=C1OCCCCC)C(OCCCCC)=C(SC1=CC=CC=C1)C(SC1=CC=CC=C1)=C5OCCCCC)C1=C3C(OCCCCC)=C(SC2=CC=CC=C2)C(SC2=CC=CC=C2)=C1OCCCCC

InChIKey

InChIKey=VAJSHRNBAQWKMO-UHFFFAOYSA-N

Formula

C120H128CuN8O8S8

Mass

2130.42

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Tetrapyrroles and derivatives

Subclass

Phthalocyanines

Intermediate Tree Nodes

Not available

Direct Parent

Phthalocyanines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phthalocyanine skeleton - Diarylthioether - Isoindole - Isoindole or derivatives - Aryl thioether - Thiophenol ether - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Pyrrole - Heteroaromatic compound - Organic transition metal salt - Sulfenyl compound - Azacycle - Thioether - Ether - Organic nitrogen compound - Organic zwitterion - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic salt - Organic copper salt - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phthalocyanines. These are cyclic tetrapyrroles that contain a phthalocyanine skeleton, which consists of four isoindole-type units, with the connecting carbon atoms in the macrocycle replaced by nitrogen.

External Descriptors

Not available

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